Medical Technology Jobs

137 jobs for “Regulatory Affairs Manager”

Results

Johnson & Johnson MedTech logo

Johnson & Johnson MedTech · 10000+ people · Public

Sales Lead East EP ICE (Intracardiac Echocardiography)

  • Vienna, Austria
  • €83,400 – €134,090 pa
  • Lead · manages people

Leads the expansion of intracardiac echocardiography (ICE) in electrophysiology across West EMEA, translating regional strategy into country growth plans and account-level execution. Manages a team of six EP ultrasound clinical specialists while partnering with country commercial, marketing, education and market access teams. Combines commercial leadership, strategic account development and launch readiness for the ICE and CARTOSOUND portfolio.

CARTOSOUND

5 days ago
Johnson & Johnson MedTech logo

Johnson & Johnson MedTech · 10000+ people · Public

Sales Lead East EP ICE (Intracardiac Echocardiography)

  • Hamburg, Germany
  • €79,100 – €127,650 pa
  • Lead · manages people

Leads the expansion of intracardiac echocardiography (ICE) in electrophysiology across West EMEA, translating regional strategy into country growth plans and account-level execution. Manages a team of six EP clinical specialists, working with country commercial teams, marketing, professional education and health economics to drive adoption, protect existing accounts and win new ones. Combines commercial leadership, strategic account development and cross-functional matrix collaboration.

CARTOSOUND

5 days ago
Newton Colmore logo

Newton Colmore · 11–50 people

Medical Devices Project Leader

  • Cambridge
  • Lead

Lead cross-functional teams through the full medical device product lifecycle, from concept to commercialisation, in a multidisciplinary Cambridge environment. The role involves managing timelines and budgets, navigating regulatory pathways, and mentoring junior staff while engaging hands-on with design teams.

2 weeks ago
Newton Colmore logo

Newton Colmore · 11–50 people

Optical Systems Engineer - Medical Devices

  • Cambridge

Hands-on role designing and integrating optical systems into complex medical devices, from early feasibility through to product launch. You'll work in a multidisciplinary team spanning simulation, prototyping, testing and refinement, with a strong emphasis on regulatory compliance and real-world usability, and mentor junior colleagues.

2 weeks ago

L-ev8 Recruitment Ltd

Quality Coordinator

  • Burgess Hill
  • On-site
  • £32,000 – £40,000 pa

Coordinating quality processes, managing non-conformances, supporting investigations and corrective actions, and maintaining ISO 9001 and ISO 13485 compliance. Reporting to the Head of Quality, the role covers document control, CAPA, supplier quality and audit support within a regulated packaging business, with scope to broaden experience across auditing and regulatory compliance.

Microsoft Office

3 weeks ago

Omega Resource Group

Quality Engineer

  • Gloucester
  • On-site
  • £45,000 – £50,000 pa
  • Mid-level
  • Permanent

Support and maintain the effectiveness of a medical device manufacturer's QMS in line with ISO 13485, MDR and FDA requirements. Day-to-day work covers CAPA effectiveness, quality data and trend analysis, non-conformances, change control and complaint investigation, plus writing and updating procedures and work instructions.

ISO 13485 · FDA Quality System

3 weeks ago

Clearline Recruitment Ltd

Clinical Study Start Up Lead

  • Welwyn Garden City
  • Hybrid · 2–3 days in office
  • £339 – £500 pd
  • Lead
  • Contract

Country and site-facing role coordinating UK clinical trial start-up through to site activation, managing regulatory submissions, approvals and amendments with the HRA, Ethics and MHRA. Involves liaising with NHS R&D departments, clinical sites and CROs, negotiating site contracts, budgets and costing templates, and tracking timelines and regulatory milestones. Requires recent hands-on UK study start-up experience and knowledge of IRAS, CPMS, iCT and ARSAC.

IRAS · CPMS · iCT +4

3 weeks ago

Planet Recruitment

Technical Publications Administrator

  • Abingdon
  • On-site
  • £28,000 – £35,000 pa
  • Permanent

Create, maintain and publish technical documentation including Instructions for Use, service manuals, production procedures and product artwork for medical devices. Work with engineering, quality and production teams to verify technical information, manage change control and prepare files for printing. Involves desktop publishing, technical illustrations and coordinating external translations.

Microsoft Word · Microsoft Excel · Adobe InDesign +3

2 weeks ago

KO2 Embedded Recruitment Solutions

Contract Medical Device Test Technician

  • Saffron Walden
  • £30 – £33 ph
  • Contract

Hands-on testing and validation of medical devices, including stress and force testing in a lab environment. The role involves analysing data for design verification, developing new test procedures, and documenting all technical activity to regulatory and quality standards. It sits within a test team on a high-impact medical device project.

2 weeks ago

Randstad Delivery

Complaints Investigator - Night Shift

  • Witney
  • On-site
  • £17 ph
  • Temporary · Shift work

Investigates returned medical devices to identify root causes of complaints, using internal systems and Excel to track trends and ensure regulatory compliance. Collaborates with international colleagues on quality improvements and pre-launch readiness for new products. Night shift role (4 on, 4 off, 7pm-7am) with full training provided, distinct from customer service.

Excel · Word

3 weeks ago

Matchtech

Quality Engineer (Medical Devices)

  • Fareham
  • Hybrid
  • Mid-level
  • Permanent

Maintains and improves a medical device Quality Management System, planning and reporting internal audits and leading external audit readiness with evidence packs and follow-up actions. Supports ISO 13485 compliance, ISO 14971 risk activities, CAPA and document control, and leads quality improvement projects in a regulated scale-up environment.

Last month

Spire Healthcare

Medical Devices Lead

  • Elland
  • On-site
  • Lead
  • Part time

Operational lead for the hospital's medical device management programme, acting as subject matter expert for equipment lifecycle, maintenance, asset control and regulatory compliance. Day to day involves managing biomedical equipment work orders, liaising with clinical departments and third-party engineers, training staff and running asset tagging and quarantine checks.

SAP · Microsoft Word · Microsoft Excel

Last month
Philips logo

Philips · 10000+ people · Public

Field Service Engineer - South East

  • United Kingdom - Remote Based
  • Remote
  • Mid-level
  • Permanent

You will install, maintain, troubleshoot and repair advanced MRI systems for customers across South East England, working independently and within a regional team. The role covers corrective and preventative maintenance, upgrades and on-call support, with opportunities to develop expertise in other imaging modalities.

Philips MRI · Philips Quality Management System

Clearance required 4 months ago
Philips logo

Philips · 10000+ people · Public

Clinical Applications Specialist (Monitoring Analytics) - London & South-Central region

  • Farnborough
  • Remote
  • £40,460 – £63,580 pa

Field-based role training hospital staff, technicians and operators on Philips monitoring and ECG equipment across London and South-Central. You run application training schedules, support product launches and demos, and feed customer feedback back to the business unit while working with Account and Product Managers.

Philips Healthcare

Last month

Adecco · 10000+ people · Public

Digital Health Strategist

  • Surrey
  • Hybrid
  • £200 – £300 pd
  • Mid-level
  • Contract

Supports a global pharmaceutical organisation's digital health strategy by identifying and evaluating early-stage opportunities that combine digital technology with healthcare products. Day to day involves market research, business case and value proposition development, external partner assessment, and Agile activities such as sprint planning and OKR reviews, working with commercial, medical, technology and brand teams.

Last month

Get new Regulatory Affairs Manager roles by email. One email a week when new roles match, or daily if you prefer. Stop any time.

Filters

Are you sure?